Bioserenity is one of 275 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Bioserenity - FDA 510(k) Cleared Devices
Recent clearances: Neuronaute with IceCap 2 & IceCap 2 Small, NEURONAUTE
2
Total
2
Cleared
0
Denied
Bioserenity has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.
Last cleared in 2023. Active since 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Bioserenity Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Voisin Consulting Inc., Life Sciences as regulatory consultant.
FDA 510(k) Regulatory Record - Bioserenity
2 devices